Circulating levels of VEGFR-1 and VEGFR-2 in patients with metastatic melanoma treated with chemoimmunotherapy alone or combined with bevacizumab

Pia P. Vihinen, Susan Ramadan, Meri Sisko Vuoristo, Micaela Hernberg, Kristiina Tyynelä-Korhonen, Tanja Skyttä, Ilkka Koskivuo, Pirkko Liisa Kellokumpu-Lehtinen, Kari Syrjänen, Seppo Pyrhönen

Research output: Contribution to journalArticleScientificpeer-review

4 Citations (Scopus)

Abstract

There are no identified biomarkers that could predict response to antiangiogenic or traditional chemoimmunotherapy in metastatic melanoma. We hypothesized that soluble angiogenic factor receptors might help us to identify patients responsive to treatment. A series of 48 patients with stage IV melanoma participating in two phase II clinical trials were included. The trials included treatment with carboplatin, vinorelbine, and subcutaneous interleukin-2 (n=22) or treatment with bevacizumab, dacarbazine, and low-dose interferon-α2a (n=26).Serum samples were prospectively collected and soluble vascular endothelial growth factor receptor 1 (s-VEGFR-1) and 2 (s-VEGFR-2) were measured before starting the trial treatment and during response evaluation.There was a trend toward longer overall survival among patients with higher-than-median serum VEGFR-1 levels (21.3 months) compared with 12.3 months in patients with low pretreatment s-VEGFR-1 levels (P=0.146). Pretreatment s-VEGFR-2 levels did not correlate to survival. Serum VEGFR-2 levels decreased during therapy in 44% of the patients and increased in 56% of the patients. VEGFR-2 increased in 78% (14 of 18) of the patients who progressed during therapy (P=0.017). VEGFR-2 decrease was associated with clinical benefit in 65% of the patients (11 of 17) and with progression in only four patients (P=0.016).High pretreatment levels of s-VEGFR-1 are associated with improved prognosis among patients with metastatic melanoma independently on therapy, whereas increased VEGFR-2 levels during therapy are associated with disease progression. These markers might be useful in selecting patients responsive to antiangiogenic therapy.

Original languageEnglish
Pages (from-to)431-437
Number of pages7
JournalMELANOMA RESEARCH
Volume21
Issue number5
DOIs
Publication statusPublished - 2011
Publication typeA1 Journal article-refereed

Keywords

  • angiogenesis
  • bevacizumab
  • chemotherapy
  • fibroblast growth factor
  • immunotherapy
  • melanoma
  • metastatic
  • prognosis
  • survival
  • vascular endothelial growth factor receptor

Publication forum classification

  • No publication forum level

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